- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05206253
Effectiveness of Egg Versus Whey Protein Powder During Resistance Training
May 24, 2024 updated by: Phil Chilibeck, University of Saskatchewan
Egg Versus Whey Protein as the Optimal Supplement for Fitness-conscious People
Consumption of whole eggs has recently been shown to stimulate muscle protein synthesis to a greater degree than consumption of egg whites after a resistance training session.
It is theorized that the egg yoke contains bio-active nutrients that enhance the protein provided by egg whites.
The study will evaluate the effect of whole egg powder compared to whey protein powder and placebo over 12 weeks of resistance training in men and women who are participating in resistance training programs.
Study Overview
Status
Completed
Conditions
Detailed Description
Consuming whole eggs after resistance training sessions appears to be more effective for simulating muscle protein synthesis that simply consuming egg whites.
The egg yolks might enhance the effect of protein derived from egg whites.
The study will compare post-exercise supplementation with about 30 grams of protein derived from whole egg powder versus whey protein powder and placebo (maltodextrin) over a 12-week resistance training program.
Resistance-trained men and women (n=120) will be randomized to consume either the whole-egg powder, whey protein powder or maltodextrin after resistance training 6 times per week for 12 weeks.
The primary outcome measure is change in lean tissue mass.
Secondary measures include change in fat mass, change in arm and leg muscle thickness, change in bench press, squat, and knee extension strength, and change in fasting blood glucose.
Study Type
Interventional
Enrollment (Actual)
115
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Saskatchewan
-
Regina, Saskatchewan, Canada, S4S 0A2
- University of Regina
-
Saskatoon, Saskatchewan, Canada, S7N5B2
- University of Saskatchewan
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 35 years (Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Resistance training experience for at least one year
Exclusion Criteria:
- Having taken any nutritional supplements the past 30 days
- Currently using anabolic steroids
- Currently taking corticosteroids
- Allergies to dairy or egg products
- Identifying any medical conditions as determined by the "Get Active Questionnaire"
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Whole egg powder
Dietary supplementation with whole egg powder after resistance training sessions
|
Nutritional supplementation during a 12 week resistance training program
|
|
Active Comparator: Whey protein powder
Dietary supplementation with whey protein powder after resistance training sessions
|
Nutritional supplementation during a 12 week resistance training program
|
|
Placebo Comparator: Maltodextrin placebo
Dietary supplementation with maltodextrin placebo after resistance training sessions
|
Nutritional supplementation during a 12 week resistance training program
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in lean tissue mass
Time Frame: 12 weeks
|
Lean tissue mass measured by DXA
|
12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in fat mass
Time Frame: 12 weeks
|
Fat mass measured by DXA
|
12 weeks
|
|
Change in biceps muscle thickness
Time Frame: 12 weeks
|
biceps muscle thickness measured by ultrasound
|
12 weeks
|
|
Change in triceps muscle thickness
Time Frame: 12 weeks
|
triceps muscle thickness measured by ultrasound
|
12 weeks
|
|
Change in quadriceps muscle thickness
Time Frame: 12 weeks
|
quadriceps muscle thickness measured by ultrasound
|
12 weeks
|
|
Change in hamstrings muscle thickness
Time Frame: 12 weeks
|
hamstrings muscle thickness measured by ultrasound
|
12 weeks
|
|
Change in bench press strength
Time Frame: 12 weeks
|
Bench press strength (kg)
|
12 weeks
|
|
Change in leg squat strength
Time Frame: 12 weeks
|
Leg squat strength (kg)
|
12 weeks
|
|
Change in knee extension strength
Time Frame: 12 weeks
|
Isokinetic knee extension torque
|
12 weeks
|
|
Change in fasting glucose
Time Frame: 12 weeks
|
Fasting glucose
|
12 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Philip Chilibeck, Ph.D., University of Saskatchewan
- Principal Investigator: Darren Candow, Ph.D., University of Regina
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 30, 2022
Primary Completion (Actual)
August 31, 2023
Study Completion (Actual)
August 31, 2023
Study Registration Dates
First Submitted
January 11, 2022
First Submitted That Met QC Criteria
January 11, 2022
First Posted (Actual)
January 25, 2022
Study Record Updates
Last Update Posted (Actual)
May 29, 2024
Last Update Submitted That Met QC Criteria
May 24, 2024
Last Verified
May 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Bio 2962
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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